cross-electrophile_coupling

Ketones from Nickel‐Catalyzed Decarboxylative, Non‐Symmetric Cross‐Electrophile Coupling of Carboxylic Acid Esters

[Weix]

[1]

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  • J. Wang, B.P. Cary, P.D. Beyer, S.H. Gellman, and D.J. Weix, "Ketones from Nickel‐Catalyzed Decarboxylative, Non‐Symmetric Cross‐Electrophile Coupling of Carboxylic Acid Esters", Angewandte Chemie International Edition, vol. 58, pp. 12081-12085, 2019. http://dx.doi.org/10.1002/anie.201906000
  • Deaminative Reductive Cross-Electrophile Couplings of Alkylpyridinium Salts and Aryl Bromides

    [1]

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  • J. Liao, C.H. Basch, M.E. Hoerrner, M.R. Talley, B.P. Boscoe, J.W. Tucker, M.R. Garnsey, and M.P. Watson, "Deaminative Reductive Cross-Electrophile Couplings of Alkylpyridinium Salts and Aryl Bromides", Organic Letters, vol. 21, pp. 2941-2946, 2019. http://dx.doi.org/10.1021/acs.orglett.9b01014
  • Stereoselective Preparation of a-C-Vinyl/Aryl Glycosides via Nickel-Catalyzed Reductive Coupling of Glycosyl Halides with Vinyl and Aryl Halides


    [1]

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  • J. Liu, and H. Gong, "Stereoselective Preparation of α-C-Vinyl/Aryl Glycosides via Nickel-Catalyzed Reductive Coupling of Glycosyl Halides with Vinyl and Aryl Halides", Organic Letters, vol. 20, pp. 7991-7995, 2018. http://dx.doi.org/10.1021/acs.orglett.8b03567
  • isible-Light-Driven External-Reductant-Free Cross-Electrophile Couplings of Tetraalkyl Ammonium Salts


    [1]

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  • L. Liao, G. Cao, J. Ye, G. Sun, W. Zhou, Y. Gui, S. Yan, G. Shen, and D. Yu, "Visible-Light-Driven External-Reductant-Free Cross-Electrophile Couplings of Tetraalkyl Ammonium Salts", Journal of the American Chemical Society, vol. 140, pp. 17338-17342, 2018. http://dx.doi.org/10.1021/jacs.8b08792
  • Synthesis of (+)-Vitepyrroloid A and (+)-Vitepyrroloid B by Late-Stage Ni-Catalyzed C(sp2)–C(sp3) Cross-Electrophile Coupling


    [1]

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  • M. Menger, D. Lentz, and M. Christmann, "Synthesis of (+)-Vitepyrroloid A and (+)-Vitepyrroloid B by Late-Stage Ni-Catalyzed C(sp2)–C(sp3) Cross-Electrophile Coupling", The Journal of Organic Chemistry, vol. 83, pp. 6793-6797, 2018. http://dx.doi.org/10.1021/acs.joc.8b00882
  • Nickel-Catalyzed Reductive Cross-Coupling of Aryl Halides with Monofluoroalkyl Halides for Late-Stage Monofluoroalkylation



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  • J. Sheng, H. Ni, H. Zhang, K. Zhang, Y. Wang, and X. Wang, "Nickel-Catalyzed Reductive Cross-Coupling of Aryl Halides with Monofluoroalkyl Halides for Late-Stage Monofluoroalkylation", Angewandte Chemie International Edition, vol. 57, pp. 7634-7639, 2018. http://dx.doi.org/10.1002/anie.201803228
  • Coupling of Challenging Heteroaryl Halides with Alkyl Halides via Nickel-Catalyzed Cross-Electrophile Coupling

    Pfizer, Asymchem & Weix

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  • E.C. Hansen, C. Li, S. Yang, D. Pedro, and D.J. Weix, "Coupling of Challenging Heteroaryl Halides with Alkyl Halides via Nickel-Catalyzed Cross-Electrophile Coupling", The Journal of Organic Chemistry, vol. 82, pp. 7085-7092, 2017. http://dx.doi.org/10.1021/acs.joc.7b01334